Variant report

Variant	nsv8872
Chromosome Location	chr11:107228364-107249620
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:107240708-107240809	K562	blood:	n/a	n/a
2	ATF2	chr11:107241054-107241483	GM12878	blood:	n/a	n/a
3	CTCF	chr11:107233572-107233629	Kidney_OC	kidney:	n/a	n/a
4	CTCF	chr11:107244188-107244259	GM10248	blood:	n/a	n/a
5	EBF1	chr11:107241262-107241305	GM12878	blood:	n/a	n/a
6	FOS	chr11:107241063-107241412	MCF10A-Er-Src	breast:	n/a	chr11:107241238-107241247 chr11:107241234-107241245 chr11:107241236-107241248 chr11:107241239-107241246 chr11:107241236-107241247 chr11:107241237-107241247 chr11:107241238-107241246
7	FOS	chr11:107241068-107241494	MCF10A-Er-Src	breast:	n/a	chr11:107241238-107241247 chr11:107241234-107241245 chr11:107241236-107241248 chr11:107241239-107241246 chr11:107241236-107241247 chr11:107241237-107241247 chr11:107241238-107241246
8	FOS	chr11:107241009-107241427	MCF10A-Er-Src	breast:	n/a	chr11:107241238-107241247 chr11:107241234-107241245 chr11:107241236-107241248 chr11:107241239-107241246 chr11:107241236-107241247 chr11:107241237-107241247 chr11:107241238-107241246
9	FOS	chr11:107241124-107241415	HUVEC	blood vessel:	n/a	chr11:107241238-107241247 chr11:107241234-107241245 chr11:107241236-107241248 chr11:107241239-107241246 chr11:107241236-107241247 chr11:107241237-107241247 chr11:107241238-107241246
10	FOS	chr11:107241026-107241427	MCF10A-Er-Src	breast:	n/a	chr11:107241238-107241247 chr11:107241234-107241245 chr11:107241236-107241248 chr11:107241239-107241246 chr11:107241236-107241247 chr11:107241237-107241247 chr11:107241238-107241246
11	FOSL2	chr11:107241093-107241436	SK-N-SH	brain:	n/a	chr11:107241238-107241247 chr11:107241234-107241245 chr11:107241236-107241248 chr11:107241239-107241246 chr11:107241237-107241247 chr11:107241238-107241246
12	FOXA1	chr11:107240572-107241011	HepG2	liver:	n/a	n/a
13	FOXA1	chr11:107240552-107240908	HepG2	liver:	n/a	n/a
14	FOXA1	chr11:107243732-107244134	HepG2	liver:	n/a	n/a
15	FOXA2	chr11:107243578-107244314	A549	lung:	n/a	n/a
16	FOXA2	chr11:107240625-107240831	HepG2	liver:	n/a	n/a
17	FOXA2	chr11:107232651-107233340	A549	lung:	n/a	n/a
18	GATA3	chr11:107228678-107228906	SH-SY5Y	brain:	n/a	n/a
19	GATA3	chr11:107231469-107231532	SH-SY5Y	brain:	n/a	n/a
20	IKZF1	chr11:107241166-107241438	GM12878	blood:	n/a	n/a
21	MEF2A	chr11:107241201-107241533	GM12878	blood:	n/a	chr11:107241384-107241405 chr11:107241388-107241404 chr11:107241391-107241400 chr11:107241390-107241401 chr11:107241389-107241403 chr11:107241384-107241405
22	MEF2C	chr11:107241165-107241511	GM12878	blood:	n/a	chr11:107241384-107241405 chr11:107241388-107241404 chr11:107241391-107241400 chr11:107241390-107241401 chr11:107241389-107241403 chr11:107241384-107241405
23	MYC	chr11:107241180-107241393	MCF10A-Er-Src	breast:	n/a	chr11:107241237-107241246 chr11:107241238-107241247
24	NFIC	chr11:107240993-107241433	GM12878	blood:	n/a	n/a
25	NFYB	chr11:107229613-107229700	GM12878	blood:	n/a	n/a
26	POLR2A	chr11:107232837-107233153	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr11:107243619-107244044	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr11:107243779-107243982	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr11:107243240-107243312	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr11:107231607-107231731	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr11:107232159-107232356	MCF10A-Er-Src	breast:	n/a	n/a
32	POLR2A	chr11:107232783-107233017	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr11:107232533-107233078	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr11:107243748-107243995	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr11:107232820-107232834	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr11:107243279-107244215	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr11:107243806-107243911	A549	lung:	n/a	n/a
38	POLR2A	chr11:107228421-107228478	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr11:107232831-107233008	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr11:107243362-107244084	H1-hESC	embryonic stem cell:	n/a	n/a
41	RUNX3	chr11:107241168-107241529	GM12878	blood:	n/a	n/a
42	SRF	chr11:107232590-107232783	GM12878	blood:	n/a	n/a
43	STAT3	chr11:107239011-107239174	MCF10A-Er-Src	breast:	n/a	chr11:107239076-107239087
44	STAT3	chr11:107230844-107230852	MCF10A-Er-Src	breast:	n/a	n/a
45	STAT3	chr11:107231749-107231774	MCF10A-Er-Src	breast:	n/a	n/a
46	STAT3	chr11:107243023-107243035	MCF10A-Er-Src	breast:	n/a	n/a
47	STAT3	chr11:107241183-107241371	MCF10A-Er-Src	breast:	n/a	chr11:107241238-107241247 chr11:107241237-107241246
48	TAF1	chr11:107243371-107244043	H1-hESC	embryonic stem cell:	n/a	n/a
49	TAF1	chr11:107243703-107244065	H1-hESC	embryonic stem cell:	n/a	n/a
50	TAF1	chr11:107232693-107233045	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107232729-107232779	HMEC	breast:	n/a
2	chr11:107232729-107232779	NT2-D1	testis:	n/a
3	chr11:107243587-107243637	Hepatocyte	liver:	n/a
4	chr11:107232729-107232779	ECC-1	luminal epithelium:	n/a
5	chr11:107232729-107232779	HRE	kidney:	n/a
6	chr11:107232729-107232779	Hela-S3	cervix:	n/a
7	chr11:107232729-107232779	HRCEpiC	kidney:	n/a
8	chr11:107232729-107232779	GM19239	blood:	n/a
9	chr11:107243587-107243637	PrEC	prostate:	n/a
10	chr11:107232729-107232779	PFSK-1	brain:	n/a
11	chr11:107243587-107243637	HRE	kidney:	n/a
12	chr11:107243587-107243637	HPAEpiC	pulmonary alveolar:	n/a
13	chr11:107232729-107232779	HCT-116	colon:	n/a
14	chr11:107243587-107243637	GM06990	blood:	n/a
15	chr11:107243587-107243637	SK-N-MC	brain:	n/a
16	chr11:107232729-107232779	BJ	skin:	n/a
17	chr11:107243587-107243637	GM12878	blood:	n/a
18	chr11:107232729-107232779	AG04450	lung:	fetal
19	chr11:107243587-107243637	HEK293	kidney:	embryo
20	chr11:107232729-107232779	Jurkat	blood:	n/a
21	chr11:107243587-107243637	AG04449	skin:	fetal
22	chr11:107243587-107243637	HepG2	liver:	n/a
23	chr11:107232729-107232779	AoSMC	blood vessel:	n/a
24	chr11:107232729-107232779	MCF10A-Er-Src	breast:	n/a
25	chr11:107243587-107243637	U87	brain:	n/a
26	chr11:107243587-107243637	AG09309	skin:	n/a
27	chr11:107232729-107232779	HL-60	blood:	n/a
28	chr11:107243587-107243637	AG04450	lung:	fetal
29	chr11:107243587-107243637	PANC-1	pancreas:	n/a
30	chr11:107232729-107232779	HepG2	liver:	n/a
31	chr11:107232729-107232779	ProgFib	skin:	n/a
32	chr11:107232729-107232779	AG10803	skin:	n/a
33	chr11:107232729-107232779	AG09319	gingival:	n/a
34	chr11:107243587-107243637	HCF	heart:	n/a
35	chr11:107243587-107243637	NT2-D1	testis:	n/a
36	chr11:107243587-107243637	GM19239	blood:	n/a
37	chr11:107243587-107243637	Hela-S3	cervix:	n/a
38	chr11:107243587-107243637	HCT-116	colon:	n/a
39	chr11:107243587-107243637	PFSK-1	brain:	n/a
40	chr11:107232729-107232779	IMR90	lung:	fetal
41	chr11:107232729-107232779	AG09309	skin:	n/a
42	chr11:107232729-107232779	CMK	blood:	n/a
43	chr11:107243587-107243637	SKMC	muscle:	n/a
44	chr11:107232729-107232779	T-47D	breast:	n/a
45	chr11:107243587-107243637	ECC-1	luminal epithelium:	n/a
46	chr11:107232729-107232779	SKMC	muscle:	n/a
47	chr11:107243587-107243637	SK-N-SH	brain:	n/a
48	chr11:107243587-107243637	HMEC	breast:	n/a
49	chr11:107243587-107243637	MCF10A-Er-Src	breast:	n/a
50	chr11:107232729-107232779	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:107241951..107244732-chr11:107327122..107328857,2	K562	blood:
2	chr11:107240491..107241393-chr16:2244600..2245300,2	MCF-7	breast:
3	chr11:107237489..107239255-chr11:107241546..107243344,2	K562	blood:
4	chr11:107237489..107239255-chr11:107241546..107243344,2	K562	blood:

Variant related genes	Relation type
CWF19L2	TF binding region
CWF19L2	CpG island
ENSG00000152404	chromatin interactions

Extended variants
information (count: 792 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:792 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191162166	chr11:107228364-107228365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs76473959	chr11:107228365-107228366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569907263	chr11:107228366-107228367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554748979	chr11:107228404-107228405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183422628	chr11:107228417-107228418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12272489	chr11:107228421-107228422	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs532338714	chr11:107228434-107228435	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs143106054	chr11:107228446-107228447	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs144209103	chr11:107228482-107228483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552338499	chr11:107228494-107228495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs686806	chr11:107228533-107228534	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs553778089	chr11:107228547-107228548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148722610	chr11:107228594-107228595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371175800	chr11:107228603-107228604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs61906000	chr11:107228657-107228658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187224239	chr11:107228658-107228659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142306632	chr11:107228704-107228705	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs190524478	chr11:107228709-107228710	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs553810439	chr11:107228719-107228720	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs537341	chr11:107228736-107228737	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs532903354	chr11:107228745-107228746	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs548097245	chr11:107228764-107228765	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs559728991	chr11:107228765-107228766	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs530019714	chr11:107228805-107228806	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs536621121	chr11:107228811-107228812	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs548683938	chr11:107228881-107228882	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs150846361	chr11:107228964-107228965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200685013	chr11:107229009-107229010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537662188	chr11:107229016-107229017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556313549	chr11:107229024-107229025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377337705	chr11:107229069-107229070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4754217	chr11:107229070-107229071	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs71044295	chr11:107229086-107229087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183153418	chr11:107229100-107229101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533703	chr11:107229136-107229137	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs533647	chr11:107229149-107229150	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs572036015	chr11:107229268-107229269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535846062	chr11:107229269-107229270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373550041	chr11:107229296-107229297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554656893	chr11:107229303-107229304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35870881	chr11:107229308-107229309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576158706	chr11:107229338-107229339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540057034	chr11:107229339-107229340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11212180	chr11:107229356-107229357	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs68000908	chr11:107229365-107229366	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs372017054	chr11:107229382-107229383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531725	chr11:107229387-107229388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377152853	chr11:107229413-107229414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577495762	chr11:107229426-107229427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11823829	chr11:107229457-107229458	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Obesity	19966786	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107169400-107230000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr11:107173600-107231400	Weak transcription	Brain Angular Gyrus	brain
3	chr11:107179200-107229800	Weak transcription	Psoas Muscle	Psoas
4	chr11:107180000-107233200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr11:107183400-107234400	Weak transcription	HSMMtube	muscle
6	chr11:107192200-107229000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:107192200-107232200	Weak transcription	Esophagus	oesophagus
8	chr11:107193800-107229800	Weak transcription	Right Ventricle	heart
9	chr11:107193800-107237200	Weak transcription	Gastric	stomach
10	chr11:107194600-107235600	Weak transcription	Aorta	Aorta
11	chr11:107195000-107299200	Weak transcription	Colon Smooth Muscle	Colon
12	chr11:107195200-107233000	Weak transcription	Fetal Muscle Trunk	muscle
13	chr11:107198200-107233200	Weak transcription	Placenta	Placenta
14	chr11:107198200-107240800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr11:107205600-107234800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr11:107214200-107232600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr11:107215400-107231200	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr11:107215800-107230000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr11:107215800-107230600	Weak transcription	Fetal Muscle Leg	muscle
20	chr11:107215800-107231600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr11:107215800-107233000	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr11:107215800-107240800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr11:107217400-107229800	Weak transcription	Lung	lung
24	chr11:107219800-107232600	Weak transcription	Duodenum Mucosa	Duodenum
25	chr11:107219800-107234800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr11:107219800-107256400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr11:107220000-107234000	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr11:107220600-107232000	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr11:107221200-107231400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr11:107221800-107229800	Weak transcription	Fetal Kidney	kidney
31	chr11:107221800-107230000	Weak transcription	Fetal Lung	lung
32	chr11:107221800-107231200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr11:107221800-107232600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr11:107221800-107232800	Weak transcription	Left Ventricle	heart
35	chr11:107221800-107258400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr11:107222000-107240200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr11:107222200-107231200	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr11:107222600-107232600	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr11:107223000-107229600	Weak transcription	Stomach Smooth Muscle	stomach
40	chr11:107223000-107253000	Weak transcription	Liver	Liver
41	chr11:107223000-107253600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr11:107223000-107256400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr11:107223000-107260600	Weak transcription	Brain Anterior Caudate	brain
44	chr11:107223000-107260600	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr11:107223200-107229800	Weak transcription	Primary T cells from cord blood	blood
46	chr11:107223200-107229800	Weak transcription	Ovary	ovary
47	chr11:107223200-107234200	Weak transcription	Rectal Smooth Muscle	rectum
48	chr11:107223200-107234800	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr11:107223600-107229600	Weak transcription	Primary B cells from cord blood	blood
50	chr11:107223600-107232200	Weak transcription	Rectal Mucosa Donor 29	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links